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3-Benzoyl-2,2,5-triphenyl-2,3-dihydro-[1,3,4]oxadiazole is a complex organic compound with the molecular formula C27H19N2O2. It is characterized by a unique structure that includes a benzoyl group attached to a 2,3-dihydro-[1,3,4]oxadiazole ring, which is further substituted with three phenyl groups. 3-benzoyl-2,2,5-triphenyl-2,3-dihydro-[1,3,4]oxadiazole is of interest in the field of organic chemistry, particularly for its potential applications in the synthesis of pharmaceuticals and materials science. The compound's properties, such as its stability and reactivity, make it a valuable candidate for further research and development in these areas.

2693-34-7

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2693-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2693-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,9 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2693-34:
(6*2)+(5*6)+(4*9)+(3*3)+(2*3)+(1*4)=97
97 % 10 = 7
So 2693-34-7 is a valid CAS Registry Number.

2693-34-7Relevant academic research and scientific papers

UNEXPECTED REACTIVITY OF THE ANION DERIVED FROM BENZOPHENONE BENZOYLHYDRAZONE IN PRESENCE OF ELECTROPHILES

Armesto, Diego,Gallego, Mar G.,Horspool, William M.,Ramos, Ana

, p. 3581 - 3584 (2007/10/02)

The reactions of the anion of benzophenone benzoylhydrazone with acid chlorides are described.These afford dihydro-oxadiazoles.In the abscence of acid chlorides the anion from the benzoylhydrazone yields open chain products such as enol ethers and N-methyl amides.An electron transfer mechanism is proposed to account for this change in behaviour.

NOTES ON THE REACTIONS OF KETONE ACYLHYDRAZONES UNDER ACYLATION CONDITIONS

Somogyi, L

, p. 5187 - 5190 (2007/10/02)

The reactions of the acetophenone and fluorenone acylhydrazones under acylation conditions were investigated.The structures of the diacylhydrazones and 1,3,4-oxadiazolines formed were proved by UV, IR, (1)H- and (13)C-NMR spectroscopical as well as by MS

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